These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

634 related items for PubMed ID: 15365985

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. The neuropathological spectrum of neurodegenerative tauopathies.
    Tolnay M, Probst A.
    IUBMB Life; 2003 Jun; 55(6):299-305. PubMed ID: 12938731
    [Abstract] [Full Text] [Related]

  • 4. Pick's complex and FTDP-17.
    Kertesz A.
    Mov Disord; 2003 Sep; 18 Suppl 6():S57-62. PubMed ID: 14502657
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Tau gene mutations and their effects.
    Goedert M.
    Mov Disord; 2005 Aug; 20 Suppl 12():S45-52. PubMed ID: 16092090
    [Abstract] [Full Text] [Related]

  • 7. [Japanese contribution to the understanding of frontotemporal dementia and parkinsonism linked to chromosome 17(FTDP-17)].
    Tsuboi Y, Wszolek ZK, Mizuno Y, Kobayashi T, Yasuda M, Yamada T.
    No To Shinkei; 2003 Feb; 55(2):107-19. PubMed ID: 12684990
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease.
    Zarranz JJ, Ferrer I, Lezcano E, Forcadas MI, Eizaguirre B, Atarés B, Puig B, Gómez-Esteban JC, Fernández-Maiztegui C, Rouco I, Pérez-Concha T, Fernández M, Rodríguez O, Rodríguez-Martínez AB, de Pancorbo MM, Pastor P, Pérez-Tur J.
    Neurology; 2005 May 10; 64(9):1578-85. PubMed ID: 15883319
    [Abstract] [Full Text] [Related]

  • 10. Phenotypic heterogeneity within a new family with the MAPT p301s mutation.
    Yasuda M, Nakamura Y, Kawamata T, Kaneyuki H, Maeda K, Komure O.
    Ann Neurol; 2005 Dec 10; 58(6):920-8. PubMed ID: 16240366
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Genetic analysis of MAPT haplotype diversity in frontotemporal dementia.
    Laws SM, Friedrich P, Diehl-Schmid J, Müller J, Ibach B, Bäuml J, Eisele T, Förstl H, Kurz A, Riemenschneider M.
    Neurobiol Aging; 2008 Aug 10; 29(8):1276-8. PubMed ID: 17386961
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Tau protein and neurodegeneration.
    Goedert M.
    Semin Cell Dev Biol; 2004 Feb 10; 15(1):45-9. PubMed ID: 15036206
    [Abstract] [Full Text] [Related]

  • 20. [Frontotemporal dementia: tau mutations, deposition, and molecular mechanisms of neuronal cell death].
    Hasegawa M.
    Rinsho Shinkeigaku; 2004 Nov 10; 44(11):879-81. PubMed ID: 15651320
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 32.